HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Amino-3-(benzylthio)-3-methylbutan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-(Benzylthio)-3-methyl-4-nitrobutan-1-ol | HCID 57475976 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Amino-3-(benzylthio)-3-methylbutan-1-ol | HCID 57475977 | 99% |
Reaction Steps
To a mixture of lithium aluminum hydride (1.67 g) and tetrahydrofuran (30 ml) was added a solution of 3-(benzylthio)-3-methyl-4-nitrobutan-1-ol (3.00 g) in tetrahydrofuran (10 ml) over 1 hr at room temperature. The reaction mixture was stirred at room temperature for 1 hr, ethanol (10 ml) and water (6.4 ml) were added in this order, and the resulting inorganic salt was removed by filtration. The filtrate was concentrated, and the residue was dissolved in ethyl acetate, dried (MgSO4), and concentrated to give the title compound (2.62 g, yield 99%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777047B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-3cd60dcd841341fd812b8d2572c021be |
| Source note | uspto-grants-2010_08 |